Mechanistic Modeling: Does it Have a Future in Process Developmen
December 18, 2014 - Process Development Forum
The application of mechanistic models for process developmen
Viral Clearance Challenges in Bioprocessing
December 3, 2014 - BioPharm Intl.
Challenges remain for virus removal and validation.
Nov 1, 2014
By: Cynthia Challener, PhD
BioPharm International
New Era for Generic Drugs
December 3, 2014 - BioPharm Intl.
Manufacturers face regulatory overhaul, while brand-generic debates escalate over biosimilars and labeling changes.
Nov 1, 2014
Optimizing Resin Performance with Disposable Chromatography Solut
December 3, 2014 - BioPharm Intl.
Although the initial uptake of single-use chromatography solutions has been relatively slow, an increased need for higher-capacity resins and the demand
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Trends in Single-use Bioreactors
December 3, 2014 - BioPharm Intl.
Representatives from industry supplier companies address innovations, reliability, barriers to adoption, and the role of singIe-use bioreactors in biopr
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DoE Provides Benefits, but Preparation Is Necessary
November 12, 2014 - BioPharm Intl.
Nov 1, 2014
By: Cynthia Challener, PhD
BioPharm International
Volume 11, Issue 27, pp. 28-29
Setting Standards for Biotech Therapeutics in India
November 12, 2014 - BioPharm Intl.
The authors take a look at the past and future impact of the Indian Pharmacopoeia Commission.
By: Anurag S. Rathore, PhD, Re
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High-Throughput Process Development in an Historical Environment
November 12, 2014 - Process Development Forum
Presentations, discussions, and information-sharing on mo
A Q&A With Dr. Anurag Rathore About the Future of QbD, Part 2
October 30, 2014 - BioPharm Intl.
This two-part Q&A series with Anurag Rathore, PhD, Professor, Department of Chemical Engineering, Indian Institute of Technology, Delhi, reveals the evolutio
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Application of Quality by Design to Viral Safety
October 29, 2014 - BioPharm International
A quality-by-design approach defines a range of potential viral contaminants of source materials and can be used to effectively achieve viral clearance.
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